Canonical Allele Identifier: PA2573175771
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1421510
ClinVar RCV Id: RCV001916949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Thr1943Ile
CA394844583
NM_001040113.2:c.5828C>T